The [3 + 2] Cycloaddition Reaction of <i>N</i>-Substituted Pyrrole-2-carboxaldehydes with Arylalkenes under Copper Catalysis: Access to Dihydropyrrolizine Skeletons-Reference-Cited by-同舟云学术

The [3 + 2] Cycloaddition Reaction of N-Substituted Pyrrole-2-carboxaldehydes with Arylalkenes under Copper Catalysis: Access to Dihydropyrrolizine Skeletons

Published:2023-12-15 Issue:51 Volume:25 Page:9136-9141
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Hao Liqiang¹,Liu Xian¹,Yi Dongxu¹,Wang Yangyang¹,Yu Xiao¹,Ma Zhihong¹²,Ji Yafei¹^ORCID

Affiliation:

1. Engineering Research Center of Pharmaceutical Process Chemistry, Ministry of Education; School of Pharmacy, East China University of Science and Technology, 130 Meilong Road, Shanghai 200237, P. R. China

2. Biotalk Co., LTD, Shanghai 200090, China

Funder

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.3c03558

Reference39 articles.

1. Recent progress in the chemistry of non-monoterpenoid indole alkaloids

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3. Chlorizidine, a Cytotoxic 5H-Pyrrolo[2,1-a]isoindol-5-one-Containing Alkaloid from a Marine Streptomyces sp.

4. Rhazinilam–Leuconolam–Leuconoxine Alkaloids from Leuconotis griffithii

5. Additional nucleotide derivatives of mitosenes. Synthesis and activity against parental and multidrug resistant L1210 leukemia

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